Particulate Metallocene-Alumoxane Catalyst

ABSTRACT

The invention relates to a process for the preparation of a particulate polyethylene product in a loop reactor, wherein the polymerization catalyst applied in the polymerization process comprises a particulate metallocene-alumoxane catalyst immobilized on a porous silica support; and whereby said metallocene-alumoxane catalyst is heterogeneously distributed on said porous silica support.

TECHNICAL FIELD OF THE INVENTION

The present invention relates to a process for the preparation of aparticulate polyethylene product. According to the invention,polyethylene products are prepared in a polymerization loop reactor,wherein the polymerization is catalyzed by a metallocene-alumoxanecatalyst which is heterogeneously distributed on an inert support.

BACKGROUND OF THE INVENTION

Polyethylene (PE) is synthesized by polymerizing ethylene (CH₂═CH₂)monomers. Because it is cheap, safe, stable to most environments andeasy to be processed polyethylene polymers are useful in manyapplications. According to the properties polyethylene can be classifiedinto several types, such as but not limited to LDPE (Low DensityPolyethylene), LLDPE (Linear Low Density Polyethylene), and HDPE (HighDensity Polyethylene). Each type of polyethylene has differentproperties and characteristics.

Ethylene polymerizations are frequently carried out in a loop reactorusing ethylene monomer, liquid diluent and catalyst, optionally one ormore co-monomer(s), and hydrogen. The polymerization in a loop reactoris usually performed under slurry conditions, with the produced polymerusually in a form of solid particles which are suspended in the diluent.The slurry in the reactor is circulated continuously with a pump tomaintain efficient suspension of the polymer solid particles in theliquid diluent. Polymer slurry is discharged from the loop reactor bymeans of settling legs, which operate on a batch principle to recoverthe slurry. Settling in the legs is used to increase the solidsconcentration of the slurry finally recovered as product slurry. Theproduct slurry is further discharged through heated flash lines to aflash tank, where most of the diluent and unreacted monomers are flashedoff and recycled.

Polymerization of ethylene involves the polymerization of ethylenemonomer in the reactor in the presence of a polymerization catalyst.Suitable catalysts for the preparation of polyethylene comprisechromium-type catalysts, Ziegler-Natta catalysts and metallocenecatalysts.

The use of metallocene catalysts for polymerization and copolymerizationof ethylene is a relatively recent development. Processes for producingpolyolefins in general and polyethylene in particular in the presence ofmetallocene catalysts have been described. Metallocenes are oftencombined with activating agents such as alumoxanes, to improve thecatalytic activity of the metallocene.

A supported metallocene-alumoxane polymerization catalyst essentiallycomprises an inert support or carrier such as silica, on which alumoxaneand metallocene are coated. In many applications for the production ofpolyolefins such as polyethylene, a porous support is used. Theproperties of such porous supports such as pore density or surface areagreatly influence the physicochemical characteristics of the finalpolyolefin product. An increased surface area of a porous supportcompared to a non-porous support in theory leads to an increase in boundcatalytically active sites.

Major objectives of a plant for producing polyethylene and itscopolymers include the preparation of polymers having physicalproperties within certain specifications and the optimization ofeconomical goals such as a specific catalyst consumption and theproduction rate of the plant. That is, it is desired to minimize theconsumption of catalyst per ton of produced polymer, this leading toincreased catalyst productivity and to a reduction in the amount ofcatalyst residue in the product, as well as to the maximization of theamount of polymer produced per hour.

However, although polymerization reactions in the presence ofmetallocene-alumoxane polymerization catalysts supported on poroussupports yield polymerization products with improved physico-mechanicalproperties, such as uniformity, miscibility, density or molecular weightdistribution, compared to polymerization reactions in the presence ofnon-supported catalysts, the catalyst activity of such supportedcatalysts is believed to be generally lower than the catalyst activityof non-supported catalysts. Hence, lower amounts of polymer per givenamount of catalyst can be produced in the presence of catalystssupported on porous supports than when carrying out polymerizationreactions in the presence of non-supported catalysts.

Moreover, when carrying out polymerization reactions in the presence ofcatalyst having low catalyst activity, higher amounts of catalyst haveto be used for preparing a given amount of polymer product. In viewthereof, higher amounts of catalyst may remain in the prepared polymerproducts, and hence such polymers may contain higher ash content.Especially, when using metallocene catalyst problems related toinsufficient catalyst activity, and consequences thereof in theresulting polymer products such as to elevated ash content, may occur.For applications in food packaging or dielectric materials, high ashcontent is unwarranted. In these kinds of applications removal of theash content in the polymer product needs to be carried outpost-production, for instance by applying various washing and extractiontechniques, which are costly and time-consuming.

In view of the above, many applications which make use of catalystsystems provided on porous supports still require improved catalystactivity to increase productivity of the polymerization reaction andhence to increase the amount of polymer product produced. Hence thereremains a need in the art to provide a polymerization process for makingpolyolefin resin, and in particular polyethylene resin using supportedcatalyst having improved productivity.

It is also a need in the art to improve polymerization reactions as toreduce ash content of produced polymers which can then be used invarious impurity-sensitive applications at minimal investment ofadditional cost and time.

In view of the above, it is an object of the present invention toprovide a polymerization process for making polyolefin resin using asupported catalyst having improved activity. It is in particular anobject to provide a polymerization process for making polyethylene usinga supported metallocene-alumoxane catalyst having improved activity.

SUMMARY OF THE INVENTION

The present invention provides a process for preparing polyethylene thatis carried out in the presence of a supported metallocene-alumoxanecatalyst in a loop reactor. The present process is at least in partbased on the use of a supported metallocene-alumoxane catalyst wherebythe alumoxane is heterogeneously distributed on a porous support. Theprocess according to the invention permits to prepare polyethylene bymeans of a polymerization catalyst having increased catalytic activity,and hence provides a polymerization product having acceptable propertiesand reduced ash content.

Thereto, the invention relates in a first aspect to a process forpreparing a particulate polyethylene product in a polymerization loopreactor, comprising the steps of:

-   (a) feeding ethylene monomer, a liquid hydrocarbon diluent,    optionally hydrogen, and optionally olefin co-monomer into said loop    reactor;-   (b) feeding a polymerization catalyst into said loop reactor;-   (c) polymerizing said monomer and said optionally co-monomer to    produce a polyethylene slurry in said diluent in said loop reactor;-   (d) allowing said polyethylene slurry to settle into one or more    settling legs connected to said loop reactor;-   (e) discharging the settled polyethylene slurry from said one or    more settling legs out of said loop reactor;    wherein said polymerization catalyst comprises a particulate    metallocene-alumoxane catalyst immobilized on a porous silica    support wherein said alumoxane is heterogeneously distributed.

According to an embodiment the invention provides a method wherein saidpolymerization loop reactor is a single loop reactor.

In another embodiment the invention provides a method wherein saidpolymerization loop reactor is a loop reactor of a double loop reactorconsisting of two serially connected loop reactors. In an example, saidthe invention provides a method wherein said polymerization loopreactor, as described above, is a first reactor of a double loopreactor.

The molar ratio of aluminum, provided by said alumoxane, to transitionmetal, provided by said metallocene, in said polymerization catalyst isgenerally homogenous/constant over the complete catalyst particle.Therefore, in another embodiment, the invention relates to a process forpreparing a particulate polyethylene product in a polymerization loopreactor as given above, wherein said polymerization catalyst comprises aparticulate metallocene-alumoxane catalyst immobilized on a poroussilica support wherein said metallocene is heterogeneously distributed.

The product recovered in accordance with the process according to theinvention is a granular polyethylene product, also named particulatepolyethylene product. The term “particulate” in the present contextintends to refer to particles. The catalysts which are used in theprocess according to the invention are metallocene-based catalysts,which have controlled granulometry and properties. More in particular,said metallocene-based catalysts include particulate catalystscomprising a metallocene and an alumoxane which are provided on silicaporous support.

The term “heterogeneously” distributed as used herein and as opposed to“homogenously distributed”, intends to refer to the feature that thealumoxane component of said catalyst, and thus inherently also saidmetallocene-alumoxane catalyst, is not evenly distributed throughoutsaid support. Hence the support shows areas or surfaces havingsignificantly more alumoxane, and thus also significantly moremetallocene, bound thereto than other areas or surfaces of said support.

During the polymerization process supported polymerization catalysts,such as metallocene-alumoxane catalysts which are immobilized on aninert support, become fragmented, the fragments becoming distributedthroughout the final polymer product. The amounts of the individualresidual elements relative to the total amount of polymer product arecollectively referred to as the ash content. This is an importantparameter as in many end product applications such as food packaging ordielectric materials there are limits on the acceptable amount of ash inthe polymer product. There is a demand in the art for polymer producthaving lower ash content.

It has now been found that a heterogeneous distribution of an activatingagent, in particular alumoxane, on an inert porous support, such assilica, increases catalyst activity, and hence increases the amount offinal polymer product that can be prepared with a given amount ofcatalyst.

Also, by using the present polymerization catalyst for preparing a givenamount of polymer product, lower amounts of catalyst need to be used,resulting in a lower ash content in the resulting polymer product.Hence, the resulting polymer product will have broader applicability ormore potential end uses.

According to the invention, by providing a polymerization catalysthaving a Al/Si ratio, wherein the aluminum is provided by the alumoxaneand the silicon is provided by the silica support, which is higheroutside the support than inside said support, said polymerizationcatalyst obtains increased activity. In a particular embodiment, theinvention provides a process wherein the molar ratio of aluminum,provided by said alumoxane, to silicon, provided by said support, is atleast twofold higher at the surface of said support than inside saidsupport. As used herein, the term “outside the support” can berepresented as the outer 30% of the volume of the particle, preferablythe outer 25% of the volume of the particle, more preferably the outer10% of the volume of the particle.

In yet another embodiment, the invention provides a process wherein themolar ratio of aluminum, provided by said alumoxane, to silicon,provided by said support inside of said support is comprised between 0.2and 0.8. As used herein, the term “inside the support” can berepresented as the inner 70% of the volume of the particle, preferablythe inner 50% of the volume of the particle.

In yet another embodiment, the invention provides a process wherein themolar ratio of aluminum, provided by said alumoxane, to silicon,provided by said support on the external surface of the porous supportis comprised between 0.4 and 8.

The invention also provides a process wherein said porous silica supporthas a surface area comprised between 200 and 700 m²/g.

In another embodiment, the invention provides a process, wherein saidporous silica support has a pore volume comprised between 0.5 and 3ml/g.

In yet another embodiment, the invention provides a process, whereinsaid porous silica support has an average pore diameter comprisedbetween 50 and 300 Angstrom, and for instance between 75 and 220Angstrom.

In still another embodiment, the invention provides a process, whereinthe molar ratio of aluminum, provided by said alumoxane, to transitionmetal provided by said metallocene, in said polymerization catalyst, issubstantially constant over the catalyst, and is for instance comprisedbetween 10 and 1000, and for instance between 50 and 500.

In an embodiment, the invention relates to a process as described abovewherein said metallocene has formula (I) or (II)

(Ar)₂MQ₂   (I) for non-bridged metallocenes; or

R″(Ar)₂MQ₂   (II) for bridged metallocenes

wherein each Ar is independently selected from the group consisting ofcyclopentadienyl, indenyl, tetrahydroindenyl, and fluorenyl; and whereinAr is optionally substituted with one or more substituents eachindependently selected from the group consisting of halogen, ahydrosilyl, a SiR₃ wherein R is a hydrocarbyl having 1 to 20 carbonatoms, and a hydrocarbyl having 1 to 20 carbon atoms and wherein saidhydrocarbyl optionally contains one or more atoms selected from thegroup comprising B, Si, S, O, F, Cl and P;

wherein M is a transition metal selected from the group consisting oftitanium, zirconium, hafnium and vanadium;

wherein each Q is independently selected from the group consisting ofhalogen; a hydrocarboxy having 1 to 20 carbon atoms; and a hydrocarbylhaving 1 to 20 carbon atoms wherein said hydrocarbyl optionally containsone or more atoms selected from the group comprising B, Si, S, O, F, Cland P;

wherein R″ is a bridge between the two Ar and selected from the groupconsisting of a C₁-C₂₀ alkylene, a germanium, a silicon, a siloxane, analkylphosphine and an amine, wherein said R″ is optionally substitutedwith one or more substituents each independently selected from the groupconsisting of halogen, a hydrosilyl, a SiR₃ wherein R is a hydrocarbylhaving 1 to 20 carbon atoms, and a hydrocarbyl having 1 to 20 carbonatoms, and wherein said hydrocarbyl optionally contains one or moreatoms selected from the group comprising B, Si, S, O, F, Cl and P.

In a further embodiment, the invention relates to a process as describedabove wherein said alumoxane has formula (III) or (IV)

R—(Al(R)—O)_(x)-AlR₂ (III) for oligomeric, linear alumoxanes; or

(—Al(R)—O—)_(y) (IV) for oligomeric, cyclic alumoxanes

wherein x is 1-40, y is 3-40, and each R is independently selected froma C₁-C₈ alkyl.

In a preferred embodiment, the invention relates to a process asdescribed above wherein M is zirconium. In other words, in a preferredembodiment, said metallocene comprises the transition metal zirconium.

In another preferred embodiment, the invention relates to a process asdescribed above wherein said alumoxane is methylalumoxane.

Main benefits of using the herein described polymerization catalyst in amethod of the invention include the preparation of polymers havingphysical properties within certain specifications, increased catalystproductivity, a reduction in the amount of catalyst residue in theproduct, as well as a maximization of the amount of polymer produced perhour, and improved polyethylene production rate.

In another aspect, the invention relates to a polyethylene productobtainable or obtained by carrying out the process according to thepresent invention.

With the insight to better show the characteristics of the invention,some preferred embodiments and examples are described hereafter.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 represents scanning electron microscopy (SEM) image andenergy-dispersive X-ray spectroscopy (EDX) spectra of a particulatemetallocene-alumoxane catalyst immobilized on a porous silica support;and whereby said metallocene-alumoxane catalyst is homogeneouslydistributed on said porous silica support (A): SEM image of aparticulate metallocene-alumoxane catalyst immobilized on a poroussilica support; and whereby said metallocene-alumoxane catalyst ishomogeneously distributed on said porous silica support (B) EDX linescanspectrum showing counts of Al coming from the particle illustrated in(A). (C) EDX linescan spectrum showing counts of Si coming from theparticle illustrated in (A). After normalization of each signal Al/Siwas found to be equal to 1 for the homogeneous particle.

FIG. 2 represents scanning electron microscopy (SEM) image andenergy-dispersive X-ray (EDX) spectra of a particulatemetallocene-alumoxane catalyst immobilized on a porous silica support;and whereby said metallocene-alumoxane catalyst is heterogeneouslydistributed on said porous silica support, and which is suitable to usein the present invention. (A): SEM image of a particulatemetallocene-alumoxane catalyst immobilized on a porous silica support;and whereby said metallocene-alumoxane catalyst is heterogeneouslydistributed on said porous silica support (B) EDX linescan spectrumshowing counts of Al coming from the particle illustrated in (A). (C)EDX linescan spectrum showing counts of Si coming from the particleillustrated in (A). After normalization of each signal Al/Si was foundto be equal to 2 in surface layer, (i.e. outer 30% of the volume of theparticle), and Al/Si was found to be equal to 0.2 in core of theheterogeneous particle.

FIG. 3 represents a graph illustrating the relative activity on polymerproduction of a particulate metallocene-alumoxane catalyst immobilizedon a porous silica support wherein said alumoxane is heterogeneouslydistributed on said support compared to the relative activity of aparticulate metallocene-alumoxane catalyst immobilized on a poroussilica support wherein said alumoxane is homogeneously distributed onsaid support.

DETAILED DESCRIPTION OF THE INVENTION

Before the present method and products of the invention are described,it is to be understood that this invention is not limited to particularmethods, components, products or combinations described, as suchmethods, components, products and combinations may, of course, vary. Itis also to be understood that the terminology used herein is notintended to be limiting, since the scope of the present invention willbe limited only by the appended claims.

As used herein, the singular forms “a”, “an”, and “the” include bothsingular and plural referents unless the context clearly dictatesotherwise.

The terms “comprising”, “comprises” and “comprised of” as used hereinare synonymous with “including”, “includes” or “containing”, “contains”,and are inclusive or open-ended and do not exclude additional,non-recited members, elements or method steps. It will be appreciatedthat the terms “comprising”, “comprises” and “comprised of” as usedherein comprise the terms “consisting of”, “consists” and “consists of”.

The recitation of numerical ranges by endpoints includes all numbers andfractions subsumed within the respective ranges, as well as the recitedendpoints.

All documents cited in the present specification are hereby incorporatedby reference in their entirety.

Unless otherwise defined, all terms used in disclosing the invention,including technical and scientific terms, have the meaning as commonlyunderstood by one of ordinary skill in the art to which this inventionbelongs. By means of further guidance, term definitions are included tobetter appreciate the teaching of the present invention.

The present invention will now be further described. In the followingpassages, different aspects of the invention are defined in more detail.Each aspect so defined may be combined with any other aspect or aspectsunless clearly indicated to the contrary. In particular, any featureindicated as being preferred or advantageous may be combined with anyother feature or features indicated as being preferred or advantageous.

Reference throughout this specification to “one embodiment” or “anembodiment” means that a particular feature, structure or characteristicdescribed in connection with the embodiment is included in at least oneembodiment of the present invention. Thus, appearances of the phrases“in one embodiment” or “in an embodiment” in various places throughoutthis specification are not necessarily all referring to the sameembodiment, but may. Furthermore, the particular features, structures orcharacteristics may be combined in any suitable manner, as would beapparent to a person skilled in the art from this disclosure, in one ormore embodiments. Furthermore, while some embodiments described hereininclude some but not other features included in other embodiments,combinations of features of different embodiments are meant to be withinthe scope of the invention, and form different embodiments, as would beunderstood by those in the art. For example, in the following claims,any of the claimed embodiments can be used in any combination.

The present invention relates to a process for the preparation of aparticulate polyethylene product in a loop reactor, comprising the stepsof polymerizing ethylene monomer in the presence of a polymerizationcatalyst whereby said polymerization catalyst comprises a particulatemetallocene-alumoxane catalyst immobilized on a porous support. Inparticular, the invention provides a process for preparing a particulatepolyethylene product in a polymerization loop reactor, comprising thesteps of:

-   -   (a) feeding ethylene monomer, a liquid hydrocarbon diluent,        optionally hydrogen, and optionally olefin co-monomer into said        loop reactor;    -   (b) feeding a polymerization catalyst into said loop reactor;    -   (c) polymerizing said monomer and said optionally co-monomer to        produce a polyethylene slurry in said diluent in said loop        reactor;    -   (d) allowing said polyethylene slurry to settle into one or more        settling legs connected to said loop reactor;    -   (e) discharging the settled polyethylene slurry from said one or        more settling legs out of said loop reactor;        wherein said polymerization catalyst comprises a particulate        metallocene-alumoxane catalyst immobilized on a porous support        wherein said alumoxane is heterogeneously distributed on said        support. The process is thus in particular characterized in that        said alumoxane is heterogeneously distributed on said support.        The polymerization catalyst as described herein preferably is a        free-flowing and particulate catalyst structure in a form        comprising dry particles.

The support or carrier is an inert organic or inorganic solid, which ischemically unreactive with any of the components of the conventionalmetallocene catalyst. Suitable support materials for the supportedcatalyst of the present invention include solid inorganic oxides, suchas silica, alumina, magnesium oxide, titanium oxide, thorium oxide, aswell as mixed oxides of silica and one or more Group 2 or 13 metaloxides, such as silica-magnesia and silica-alumina mixed oxides. Silica,alumina, and mixed oxides of silica and one or more Group 2 or 13 metaloxides are preferred support materials. Preferred examples of such mixedoxides are the silica-aluminas. Most preferred is silica. The silica maybe in granular, agglomerated, fumed or other form.

Prior to its use, if desired, the support material may be subjected to aheat treatment and/or chemical treatment to reduce the water content orthe hydroxyl content of the support material. Typical thermalpretreatments are carried out at a temperature from 30 to 1000° C. for aduration of 10 minutes to 50 hours in an inert atmosphere or underreduced pressure.

A porous support as provided herein can be considered as comprising amacroscopic (i.e. visible) external surface including the surface of anymacrospores; and a (non visible) internal surface, i.e. the surface ofpores provided inside said support. According to the invention, thealumoxane is not homogeneously distributed on the porous support. Morealumoxane is present on certain areas of the porous support than onother areas of the porous support, i.e. the alumoxane concentration isheterogeneous or not uniform on the porous support. It is in particularpreferred that the alumoxane be present in a substantially higherconcentration “outside” the support than “inside” the support. By“inside” the support we mean the internal surface area of the support,including the surface lining the pores inside the support. “Inside” istherefore also used as synonym for the expressions “in the pores” of theporous support, or “inner pores” of the porous support. By “outside” thesupport we mean on the external surface of the support and the surfaceof any macropores. “Outside” is herein also used as synonym for the“external surface” or the “outer surface” of the porous support.

The concentration or distribution of alumoxane on the inside and theoutside of the support can be expressed as the molar aluminum/siliconratio or molar Al/Si ratio. This is the molar amount of aluminum permole silicon. The molar amount of aluminum equals the molar amount ofalumoxane. The molar amount of silicon equals the molar amount ofsilica. In an embodiment, the molar Al/Si ratio on the external surfaceof the porous support is at least twofold, and for instance at least 5,10 or 20 fold the molar Al/Si ratio inside said support, i.e. in thepores of the porous support.

In an embodiment, the molar Al/Si ratio in the pores of the poroussupport is comprised between 0.2 and 0.8. In a non-limiting example, themolar Al/Si ratio in the pores of the porous support is 0.2, 0.3, 0.4,0.5, 0.6, 0,7, or 0.8.

In another embodiment, the molar Al/Si ratio on the external surface ofthe porous support is comprised between 0.4 and 8, and for instancebetween 1.5 and 5.

The location or distribution of particles, such as alumoxanes, on aporous support can be measured by various techniques known by a skilledperson, such as for instance Scanning ElectronMicroscope/Energy-Dispersive X-ray spectroscopy (SEM/EDX) analysis.

In other embodiments, the support of a polymerization catalyst asdefined herein has one or more of the following properties.

In an embodiment, the invention provides a process wherein the supportof the polymerization catalyst is a porous silica support having amedian particle diameter comprised between 10 and 100 μm, and preferablybetween 10 and 55 μm. The “median particle diameter” as used herein,refers to the particle diameter of the catalyst for which fifty percentof the particles has a diameter lower than the median particle diameter.The “median particle diameter” or “d50” of a catalyst as used hereinessentially refer to a same parameter and refer to the particle diameterof the catalyst for which fifty percent of the particles has a diameterlower than the d50. The catalyst's d50 is generally measured by laserdiffraction analysis on a Malvern type analyzer after having put thecatalyst in suspension in a solvent such as e.g. cyclohexane.

In an embodiment, the invention provides a process wherein the supportof the polymerization catalyst is a porous support, and preferably aporous silica support having a surface area comprised between 200 and700 m²/g, and preferably between 250 and 350 m²/g.

In another embodiment, the invention provides a process wherein thesupport of the polymerization catalyst is a porous support, andpreferably a porous silica support having an average pore volumecomprised between 0.5 and 3 ml/g, and preferably between 1 and 2 ml/g.

In yet another embodiment, the invention provides a process wherein thesupport of the polymerization catalyst is a porous support, andpreferably a porous silica support having an average pore diametercomprised between 50 and 300 Angstrom, and preferably between 75 and 220Angstrom.

Reference will now be made to the polymerization catalyst applied in theprocess according to the invention. The term “catalyst” as used herein,is defined as a substance that causes a change in the rate of a chemicalreaction without itself being consumed in the reaction. The term“polymerization catalyst” and “catalyst” may be considered herein assynonyms. The catalysts used in the invention are metallocene-basedcatalysts.

As used herein, the term “metallocene” refers to a transition metalcomplex with a coordinated structure, consisting of a metal atom bondedto one or more ligands. The metallocenes which are used according to theinvention are represented by formula (I) or (II):

(Ar)₂MQ₂   (I); or

R″(Ar)₂MQ₂   (II)

wherein the metallocenes according to formula (I) are non-bridgedmetallocenes and the metallocenes according to formula (II) are bridgedmetallocenes;

wherein said metallocene according to formula (I) or (II) has two Arbound to M which can be the same or different from each other;

wherein Ar is an aromatic ring, group or moiety and wherein each Ar isindependently selected from the group consisting of cyclopentadienyl,indenyl, tetrahydroindenyl or fluorenyl, wherein each of said groups maybe optionally substituted with one or more substituents eachindependently selected from the group consisting of halogen, ahydrosilyl, a SiR₃ group wherein R is a hydrocarbyl having 1 to 20carbon atoms, and a hydrocarbyl having 1 to 20 carbon atoms, and whereinsaid hydrocarbyl optionally contains one or more atoms selected from thegroup comprising B, Si, S, O, F, Cl and P;

wherein M is a transition metal selected from the group consisting oftitanium, zirconium, hafnium and vanadium; and preferably is zirconium;

wherein each Q is independently selected from the group consisting ofhalogen; a hydrocarboxy having 1 to 20 carbon atoms; and a hydrocarbylhaving 1 to 20 carbon atoms and wherein said hydrocarbyl optionallycontains one or more atoms selected from the group comprising B, Si, S,O, F, Cl and P; and

wherein R″ is a divalent group or moiety bridging the two Ar groups andselected from the group consisting of a C₁-C₂₀ alkylene, a germanium, asilicon, a siloxane, an alkylphosphine and an amine, and wherein said R″is optionally substituted with one or more substituents eachindependently selected from the group consisting of halogen, ahydrosilyl, a SiR₃ group wherein R is a hydrocarbyl having 1 to 20carbon atoms, and a hydrocarbyl having 1 to 20 carbon atoms and whereinsaid hydrocarbyl optionally contains one or more atoms selected from thegroup comprising B, Si, S, O, F, Cl and P.

The term “hydrocarbyl having 1 to 20 carbon atoms” as used herein isintended to refer to a moiety selected from the group comprising alinear or branched C₁-C₂₀ alkyl; C₃-C₂₀ cycloalkyl; C₆-C₂₀ aryl; C₇-C₂₀alkylaryl and C₇-C₂₀ arylalkyl, or any combinations thereof.

Exemplary hydrocarbyl groups are methyl, ethyl, propyl, butyl, amyl,isoamyl, hexyl, isobutyl, heptyl, octyl, nonyl, decyl, cetyl,2-ethylhexyl, and phenyl.

Exemplary halogen atoms include chlorine, bromine, fluorine and iodineand of these halogen atoms, fluorine and chlorine are preferred.

In accordance with the present invention, a process is provided whereinethylene monomer is polymerized in the presence of a bridged ornon-bridged metallocene. “Bridged metallocenes” as used herein, aremetallocenes in which the two aromatic transition metal ligands, denotedas Ar in formula (I) and (II) (i.e. the two cyclopentadienyl, indenyl,tetrahydroindenyl or fluorenyl groups) are covalently linked orconnected by means of a structural bridge. Such structural bridge,denoted as R″ in formula (I) and (II) imparts stereorigidity on themetallocene, i.e. the free movement of the metal ligands is restricted.According to the invention, the bridged metallocene consists of a mesoor racemic stereoisomer.

In a preferred embodiment, the metallocenes which are used in a processaccording to the invention are represented by formula (I) or (II) asgiven above,

wherein Ar is as defined above, and wherein both Ar are the same and areselected from the group consisting of cyclopentadienyl, indenyl,tetrahydroindenyl and fluorenyl, wherein each of said groups may beoptionally substituted with one or more substituents each independentlyselected from the group consisting of halogen, a hydrosilyl, a SiR₃group wherein R is a hydrocarbyl having 1 to 20 carbon atoms as definedherein, and a hydrocarbyl having 1 to 20 carbon atoms as defined herein;

wherein M is as defined above, and preferably is zirconium,

wherein Q is as defined above, and preferably both Q are the same andare selected from the group consisting of chloride, fluoride and methyl,and preferably are chloride; and

and wherein R″ when present, is as defined above and preferably isselected from the group consisting of a C₁-C₂₀ alkylene, and a silicon,and wherein said R″ is optionally substituted with one or moresubstituents each independently selected from the group consisting of ahalogen, a hydrosilyl, a SiR₃ group wherein R is a hydrocarbyl having 1to 20 carbon atoms as defined herein, and a hydrocarbyl having 1 to 20carbon atoms as defined herein.

In another preferred embodiment, the metallocenes which are used in aprocess according to the invention are represented by formula (I) or(II) as given above,

wherein Ar is as defined above, and wherein both Ar are different andare selected from the group consisting of cyclopentadienyl, indenyl,tetrahydroindenyl and fluorenyl, wherein each of said groups may beoptionally substituted with one or more substituents each independentlyselected from the group consisting of halogen, a hydrosilyl, a SiR₃group wherein R is a hydrocarbyl having 1 to 20 carbon atoms as definedherein, and a hydrocarbyl having 1 to 20 carbon atoms as defined herein;

wherein M is as defined above, and preferably is zirconium,

wherein Q is as defined above, and preferably both Q are the same andare selected from the group consisting of chloride, fluoride and methyl,and preferably are chloride; and

and wherein R″ when present is as defined above and preferably isselected from the group consisting of a C₁-C₂₀ alkylene, and a silicon,and wherein said R″ is optionally substituted with one or moresubstituents each independently selected from the group consisting of ahalogen, a hydrosilyl, a SiR₃ group wherein R is a hydrocarbyl having 1to 20 carbon atoms as defined herein, and a hydrocarbyl having 1 to 20carbon atoms as defined herein.

In an embodiment, the invention provides a process wherein saidmetallocene is ah unbridged metallocene.

In a preferred embodiment the invention provides a process wherein saidmetallocene is an unbridged metallocene of formula (I)

(Ar)₂MQ₂   (I)

wherein said two Ar that are bound to M are the same and are selectedfrom the group consisting of cyclopentadienyl, indenyl, andtetrayhydroindenyl, wherein each of said groups may be optionallysubstituted with one or more substituents each independently selectedfrom the group consisting of halogen and a hydrocarbyl having 1 to 20carbon atoms as defined herein;

wherein M is a transition metal selected from the group consisting oftitanium, zirconium, hafnium and vanadium; and preferably is zirconium;and

wherein both Q are the same and are selected from the group consistingof chloride, fluoride and methyl, and preferably are chloride.

In a preferred embodiment, the invention provides a process wherein saidmetallocene is an unbridged metallocene selected from the groupcomprising bis(iso-butylcyclopentadienyl)zirconium dichloride,bis(pentamethylcyclopentadienyl)zirconium dichloride,bis(tetrahydroindenyl)zirconium dichloride, bis(indenyl)zirconiumdichloride, bis(1,3-dimethylcyclopentadienyl)zirconium dichloride,bis(methylcyclopentadienyl)zirconium dichloride,bis(n-butylcyclopentadienyl)zirconium dichloride, andbis(cyclopentadienyl)zirconium dichloride; and preferably selected fromthe group comprising bis(cyclopentadienyl)zirconium dichloride,bis(tetrahydroindenyl)zirconium dichloride, bis(indenyl)zirconiumdichloride, and bis(n-butyl-cyclopentadienyl)zirconium dichloride.

In another embodiment, the invention provides a process wherein saidmetallocene is a bridged metallocene.

In a preferred embodiment the invention provides a process wherein saidmetallocene is an bridged metallocene of formula (II)

R″(Ar)₂MQ₂   (II)

wherein said two. Ar that are bound to M are the same and are selectedfrom the group consisting of cyclopentadienyl, indenyl, andtetrayhydroindenyl, wherein each of said groups may be optionallysubstituted with one or more substituents each independently selectedfrom the group consisting of halogen and a hydrocarbyl having 1 to 20carbon atoms as defined herein;

wherein M is a transition metal selected from the group consisting oftitanium, zirconium, hafnium and vanadium; and preferably is zirconium;

wherein both Q are the same and are selected from the group consistingof chloride, fluoride and methyl, and preferably are chloride, and

wherein R″ is selected from the group consisting of a C₁-C₂₀ alkylene,and a silicon, and wherein said R″ is optionally substituted with one ormore substituents each independently selected from the group consistingof a halogen, and a hydrocarbyl having 1 to 20 carbon atoms as definedherein.

In a preferred embodiment, the invention provides a process wherein saidmetallocene is a bridged metallocene selected from the group comprisingethylenebis(4,5,6,7-tetrahydro-1-indenyl)zirconium dichloride,ethylenebis(1-indenyl)zirconium dichloride, dimethylsilylenebis(2-methyl-4-phenyl-inden-1-yl)zirconium dichloride, dimethylsilylenebis(2-methyl-1H-cyclopenta[a]naphthalen-3-yl)zirconium dichloride,cyclohexylmethylsilylenebis[4-(4-tert-butylphenyl)-2-methyl-inden-1-yl]zirconium dichloride,dimethylsilylenebis[4-(4-tert-butylphenyl)-2-(cyclohexylmethyl)inden-1-yl]zirconiumdichloride.

In another preferred embodiment the invention provides a process whereinsaid metallocene is an bridged metallocene of formula (II)

R″(Ar)₂MQ₂   (II)

wherein said two Ar that are bound to M are different and are selectedfrom the group consisting of cyclopentadienyl and fluorenyl, whereineach of said groups may be optionally substituted with one or moresubstituents each independently selected from the group consisting ofhalogen and a hydrocarbyl having 1 to 20 carbon atoms as defined herein;

wherein M is a transition metal selected from the group consisting oftitanium, zirconium, hafnium and vanadium; and preferably is zirconium;

wherein both Q are the same and are selected from the group consistingof chloride, fluoride and methyl, and preferably are chloride, and

wherein R″ is selected from the group consisting of a C₁-C₂₀ alkylene,and a silicon, and wherein said R″ is optionally substituted with one ormore substituents each independently selected from the group consistingof a halogen, and a hydrocarbyl having 1 to 20 carbon atoms as definedherein.

In another preferred embodiment, the invention provides a processwherein said metallocene is a bridged metallocene selected from thegroup comprising diphenylmethylene (3-t-butyl-5-methyl-cyclopentadienyl)(4,6-di-t-butyl-fluorenyl)zirconium dichloride,di-p-chlorophenylmethylene(3-t-butyl-5-methyl-cyclopentadienyl)(4,6-di-t-butyl-fluorenyl)zirconiumdichloride, diphenylmethylene(cyclopentadienyl)(fluoren-9-yl)zirconiumdichloride,dimethylmethylene(cyclopentadienyl)(2,7-ditert-butyl-fluoren-9-yl)zirconiumdichloride, dimethylmethylene[1-(4-tert-butyl-2-methyl-cyclopentadienyl)](fluoren-9-yl)zirconiumdichloride, diphenylmethylene[1-(4-tert-butyl-2-methyl-cyclopentadienyl)](2,7-ditert-butyl-fluoren-9-yl)zirconium dichloride, dimethylmethylene[1-(4-tert-butyl-2-methyl-cyclopentadienyl)](3,6-ditert-butyl-fluoren-9-yl)zirconium dichloride anddimethylmethylene (cyclopentadienyl)(fluoren-9-yl)zirconium dichloride.

Metallocene compounds used in accordance with the present invention areimmobilized on a support in the presence of an activating agent. In apreferred embodiment, alumoxane is used as an activating agent for themetallocene. The alumoxane can be used in conjunction with a catalyst inorder to improve the activity of the catalyst during the polymerizationreaction. As used herein, the term alumoxane is used interchangeablywith aluminoxane and refers to a substance, which is capable ofactivating the metallocene.

Alumoxanes used in accordance with the present invention compriseoligomeric linear and/or cyclic alkyl alumoxanes. In an embodiment, theinvention provides a process wherein said alumoxane has formula (III) or(IV)

R—(Al(R)—O)_(x)—AlR₂   (III) for oligomeric, linear alumoxanes; or

(—Al(R)—O—)_(y)   (IV) for oligomeric, cyclic alumoxanes

wherein x is 1-40, and preferably 10-20;

wherein y is 3-40, and preferably 3-20; and

wherein each R is independently selected from a C₁-C₈ alkyl, andpreferably is methyl.

In a preferred embodiment, the alumoxane is methylalumoxane. Generally,in the preparation of alumoxanes from, for example, aluminum trimethyland water, a mixture of linear and cyclic compounds is obtained. Methodsfor manufacturing alumoxane are known in the art and will therefore notbe disclosed in detail herein.

In a particular embodiment, the invention provides a process wherein themolar ratio of aluminum, provided by the alumoxane, to transition metal,provided by the metallocene, of the polymerization catalyst is constantover the catalyst. Hence, the molar ratio of aluminum to transitionmetal is preferentially the same on the surface of the support andinside the pores of the support. In a preferred embodiment, theinvention provides a process wherein the molar ratio of aluminum,provided by the alumoxane, to transition metal, provided by themetallocene, of the polymerization catalyst is comprised between 50 and500, and for instance between 50 and 150, or between 100 and 150.

A polymerization catalyst according to the present invention can beprepared according to various methods. One method for instance comprisesdifferent successive impregnation steps of the support with thealumoxane until the pores of the support are saturated, after whichexcess alumoxane can adhere onto the surface of the support. It shallhowever be clear that other methods for preparing a polymerizationcatalyst according to the present invention may also be applied.

In a further embodiment the invention relates to a method for thepolymerization of ethylene in an ethylene polymerization loop reactor,comprising the steps of;

-   -   feeding ethylene monomer, a diluent, optionally hydrogen, and        optionally one or more co-monomer(s) to said ethylene        polymerization loop reactor;    -   feeding a polymerization catalyst into said loop reactor;    -   polymerizing said monomer and said optional co-monomer to        produce a polyethylene slurry comprising liquid diluent and        solid polyethylene particles, and    -   recovering polyethylene particles from the slurry by separating        at least a majority of the diluent from the slurry.        wherein said polymerization catalyst is as described herein.

In accordance with the invention, ethylene polymerizes in a liquiddiluent in the presence of a polymerization catalyst as defined herein,optionally a co-monomer, optionally hydrogen and optionally otheradditives, thereby producing polymerization slurry comprisingpolyethylene.

As used herein, the term “polymerization slurry”, “polyethylene slurry”or “polymer slurry” or “slurry” means substantially a multi-phasecomposition including at least polymer solids and a liquid phase, theliquid phase being the continuous phase. The solids include catalyst anda polymerized olefin, such as polyethylene. The liquids include an inertdiluent, such as isobutane, dissolved monomer such as ethylene,co-monomer, molecular weight control agents, such as hydrogen,antistatic agents, antifouling agents, scavengers, and other processadditives.

Suitable “ethylene polymerization” includes but is not limited tohomo-polymerization of ethylene or the co-polymerization of ethylene anda higher 1-olefin co-monomer such as butene, 1-pentene, 1-hexene,1-octene or 1-decene.

As used herein the term “co-monomer” refers to co-monomers which aresuitable for being polymerized with ethylene monomers. Co-monomers maycomprise but are not limited to aliphatic C₃-C₂₀ alpha-olefins. Examplesof suitable aliphatic C₃-C₂₀ alpha-olefins include propylene, 1-butene,4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene,1-tetradecene, 1-hexadecene, 1-octadecene and 1-eicosene.

Hydrocarbon diluents which are suitable for being used in accordancewith the present invention may comprise but are not limited tohydrocarbon diluents such as aliphatic, cycloaliphatic and aromatichydrocarbon solvents, or halogenated versions of such solvents. Thepreferred solvents are C₁₂ or lower, straight chain or branched chain,saturated hydrocarbons, C₅ to C₉ saturated alicyclic or aromatichydrocarbons or C₂ to C₆ halogenated hydrocarbons. Nonlimitingillustrative examples of solvents are butane, isobutane, pentane,hexane, heptane, cyclopentane, cyclohexane, cycloheptane, methylcyclopentane, methyl cyclohexane, isooctane, benzene, toluene, xylene,chloroform, chlorobenzenes, tetrachloroethylene, dichloroethane andtrichloroethane. In a preferred embodiment of the present invention,said diluent is isobutane. However, it should be clear from the presentinvention that other diluents may as well be applied according to thepresent invention.

According to another embodiment the invention provides a method whereinsaid ethylene polymerization loop reactor, as described above is asingle loop reactor.

In another embodiment the invention provides a method wherein saidethylene polymerization loop reactor, as described above is a firstreactor of a double loop reactor, i.e. a reactor consisting of twoserially connected loop reactors.

A double loop reactor configuration can be used to prepare a bimodalpolyethylene. “Bimodal polyethylene” or “bimodal polyethylene product”as used herein refers to a bimodal polyethylene resin comprising twocomponents having different properties, such as for instance twocomponents of different molecular weight; two components of differentdensities; and/or two components having different productivities orreaction rates with respect to co-monomer. In an example one of saidfractions has a higher molecular weight than said other fraction. Inanother example, one of said fractions has a higher density than saidother fraction. However, the invention is not limited to the regulationof bimodal molecular weights or densities only, but may be used forbimodal regulation of other aspects of resin products, such as, but notlimited to, co-monomer introduction, polydispersity, stereospecificity,etc.

In an embodiment, a process for the preparation of a particulate bimodalpolyethylene product in a serially connected double loop reactor isprovided, comprising the steps of:

(a) feeding ethylene monomer, a liquid hydrocarbon diluent, at least onepolymerization catalyst, optionally hydrogen, and optionally one or moreolefin co-monomers to a first loop reactor;

(b) polymerizing said ethylene and said optionally one or more olefinco-monomers in said first loop reactor to produce a first polyethyleneproduct;

(c) transferring said first polyethylene product to a second loopreactor;

(d) feeding ethylene monomer, a diluent, optionally hydrogen, andoptionally one or more olefin co-monomers to said second loop reactor;

(e) polymerizing said ethylene and said optionally one or more olefinco-monomers in said second loop reactor in the presence of said firstpolyethylene product to produce a bimodal polyethylene product;

wherein said polymerization catalyst is as defined herein and comprisesa particulate metallocene-alumoxane catalyst immobilized on a poroussilica support wherein said alumoxane is heterogeneously distributed onsaid support.

The invention further relates to polyethylene products that areobtainable or obtained by carrying out a process according to theinvention.

As used the person skilled in the art will appreciate that the nature,amounts and concentrations of the above given monomers, co-monomers,polymerization catalysts and additional compounds for the polymerizationas well as the polymerization time and reaction conditions in eachreactor can vary depending on the desired polyethylene product.

EXAMPLES

6% by weight of Ethylene monomer, with about 700 ppm in volume of H2 inthe ethylene feed were added to a reactor, together with 40 ml hexene, 1ml of alkylaluminium scavenger and about 2L of isobutane diluent. 50 mgof particulate metallocene-alumoxane catalyst immobilized on a poroussilica support wherein said alumoxane is heterogeneously distributed(referred as heterogeneous), was introduced in the reactor. Thepolymerization reaction was performed at 85° C. FIG. 2 representsscanning electron microscopy (SEM) image and energy-dispersive X-ray(EDX) spectra of a heterogeneously distributed metallocene catalystwhich could be used for this reaction.

A comparative reaction was performed using 6% by weight of Ethylenemonomer, with about 700 ppm in volume of H2 in the ethylene feed wereadded to a reactor, together with 40 ml hexene, 1 ml of alkylaluminiumscavenger and about 2 L of isobutane diluent. 50 mg of particulatemetallocene-alumoxane catalyst immobilized on a porous silica supportwherein said alumoxane is homogeneously distributed (referred ashomogeneous), was introduced in the reactor. The polymerization reactionwas performed at 85° C. FIG. 1 represents scanning electron microscopy(SEM) image and energy-dispersive X-ray (EDX) spectra of a homogeneouslydistributed metallocene catalyst which could be used for thiscomparative reaction.

The relative activity of the homogenous and heterogeneous catalysts onthe copolymerization was compared and the results are shown in FIG. 3.The relative activity of the homogenously distributed catalyst was about100 while the relative activity of the heterogeneously distributedcatalyst was about 145, showing the benefits of using the hereindescribed heterogeneously distributed polymerization catalyst in apolymerization method according to embodiments of the invention.

1-15. (canceled)
 16. A process for preparing a particulate polyethyleneproduct in a loop reactor comprising: polymerizing ethylene monomers inthe presence of a polymerization catalyst comprising a particulatemetallocene-alumoxane catalyst immobilized on a porous support, whereinthe alumoxane is heterogeneously distributed on the porous support. 17.The process of claim 16, wherein the porous support is a porous silicasupport.
 18. The process of claim 17, wherein the molar ratio ofaluminum, provided by the alumoxane, to silicon, provided by the poroussilica support, is at least twofold higher at a surface of the poroussilica support than inside the porous silica support.
 19. The process ofclaim 17, wherein the molar ratio of aluminum, provided by thealumoxane, to silicon, provided by the porous silica support inside ofthe porous silica support is between 0.2 and 0.8.
 20. The process ofclaim 17, wherein the molar ratio of aluminum, provided by thealumoxane, to silicon, provided by the porous silica support on theexternal surface of the porous silica support is between 0.4 and
 8. 21.The process of claim 16, wherein the porous support has a medianparticle diameter that is between 10 and 100 μm.
 22. The process ofclaim 16, wherein the porous support has a surface area that is between200 and 700 m²/g.
 23. The process of claim 16, wherein the poroussupport has a pore volume that is between 0.5 and 3 ml/g.
 24. Theprocess of claim 16, wherein the porous support has an average porediameter that is between 50 and 300 angstroms.
 25. The process of claim16, wherein the molar ratio of aluminum, provided by the alumoxane, totransition metal, provided by the metallocene, in the polymerizationcatalyst is between 10 and
 1000. 26. The process of claim 16, whereinthe metallocene is represented by formula (I) or formula (II):(Ar)₂MQ₂ for non-bridged metallocenes;   (I)R″(Ar)₂MQ₂ for bridged metallocenes;   (II) wherein each Ar isindependently selected from the group consisting of cyclopentadienyl,indenyl, tetrahydroindenyl, and fluorenyl; wherein Ar is optionallysubstituted with one or more substituents each substituent independentlyselected from the group consisting of halogen, a hydrosilyl, an SiR₃group wherein R is a hydrocarbyl having 1 to 20 carbon atoms, and ahydrocarbyl having 1 to 20 carbon atoms and wherein said hydrocarbyloptionally contains one or more atoms selected from the group consistingof B, Si, S, O, F, Cl, and P; wherein M is a transition metal selectedfrom the group consisting of titanium, zirconium, hafnium and vanadium;wherein each Q is independently selected from the group consisting ofhalogen, a hydrocarboxy having 1 to 20 carbon atoms, and a hydrocarbylhaving 1 to 20 carbon atoms wherein said hydrocarbyl optionally containsone or more atoms selected from the group consisting of B, Si, S, O, F,Cl and P; wherein R″ is a bridge between the two Ar and is selected fromthe group consisting of a C₁-C₂₀ alkylene, a germanium, a silicon, asiloxane, an alkylphosphine and an amine; wherein R″ is optionallysubstituted with one or more substituents each independently selectedfrom the group consisting of a halogen, a hydrosilyl, a SiR₃ groupwherein R is a hydrocarbyl having 1 to 20 carbon atoms, and ahydrocarbyl having 1 to 20 carbon atoms and wherein the hydrocarbyloptionally contains one or more atoms selected from the group consistingof B, Si, S, O, F, Cl and P.
 27. The process of claim 16, wherein thealumoxane is represented by formula (III) or formula (IV)R—(Al(R)—O)_(x)—AlR₂ for oligomeric, linear alumoxanes;   (III)(—Al(R)—O—)_(y) for oligomeric, cyclic alumoxanes;   (IV) wherein x is1-40, y is 3-40, and each R is independently selected from a C₁-C₈alkyl.
 28. The process of claim 16, wherein the alumoxane ismethylalumoxane.
 29. The process of claim 16, wherein the metallocene isheterogeneously distributed on the porous support.
 30. The process ofclaim 16, wherein the metallocene is an unbridged metallocene selectedfrom the group consisting of: bis(isobutylcyclopentadienyl)zirconiumdichloride; bis(pentamethylcyclopentadienyl)zirconium dichloride;bis(tetrahydroindenyl)zirconium dichloride; bis(indenyl)zirconiumdichloride; bis(1,3-dimethylcyclopentadienyl)zirconium dichloride;bis(methylcyclopentadienyl)zirconium dichloride;bis(n-butylcyclopentadienyl)zirconium dichloride; andbis(cyclopentadienyl)zirconium dichloride.
 31. The process of claim 16,wherein the metallocene is an unbridged metallocene selected from thegroup consisting of: bis(cyclopentadienyl)zirconium dichloride;bis(tetrahydroindenyl)zirconium dichloride; bis(indenyl)zirconiumdichloride; and bis(n-butyl-cyclopentadienyl)zirconium dichloride. 32.The process of claim 16, wherein the metallocene is a bridgedmetallocene selected from the group consisting of:ethylenebis(4,5,6,7-tetrahydro-1-indenyl)zirconium dichloride;ethylenebis(1-indenyl)zirconium dichloride; dimethylsilylenebis(2-methyl-4-phenyl-inden-1-yl)zirconium dichloride; dimethylsilylenebis(2-methyl-1H-cyclopenta[a]naphthalen-3-yl)zirconium dichloride;cyclohexylmethylsilylenebis[4-(4-tert-butylphenyl)-2-methyl-inden-1-yl]zirconium dichloride; anddimethylsilylenebis[4-(4-tert-butylphenyl)-2-(cyclohexylmethyl)inden-1-yl]zirconiumdichloride.
 33. The process of claim 16, wherein the metallocene is abridged metallocene selected from the group consisting of:diphenylmethylene(3-t-butyl-5-methyl-cyclopentadienyl)(4,6-di-t-butyl-fluorenyl)zirconiumdichloride;di-p-chlorophenylmethylene(3-t-butyl-5-methyl-cyclopentadienyl)(4,6-di-t-butyl-fluorenyl)zirconiumdichloride; diphenylmethylene(cyclopentadienyl)(fluoren-9-yl)zirconiumdichloride;dimethylmethylene(cyclopentadienyl)(2,7-ditert-butyl-fluoren-9-yl)zirconiumdichloride;dimethylmethylene[1-(4-tert-butyl-2-methyl-cyclopentadienyl)](fluoren-9-yl)zirconiumdichloride;diphenylmethylene[1-(4-tert-butyl-2-methyl-cyclopentadienyl)](2,7-ditert-butyl-fluoren-9-yl)zirconiumdichloride;dimethylmethylene[1-(4-tert-butyl-2-methyl-cyclopentadienyl)](3,6-ditert-butyl-fluoren-9-yl)zirconiumdichloride; anddimethylmethylene(cyclopentadienyl)(fluoren-9-yl)zirconium dichloride.34. A particulate polyethylene product formed by the process of claim16.
 35. A particulate polyethylene product formed by: feeding ethylenemonomer, a liquid hydrocarbon diluent, optionally hydrogen, andoptionally olefin co-monomer into a loop reactor; feeding apolymerization catalyst into the loop reactor; polymerizing the ethylenemonomer and optionally the co-monomer to produce a polyethylene slurryin the liquid hydrocarbon diluent in the loop reactor; allowing thepolyethylene slurry to settle into one or more settling legs connectedto the loop reactor; discharging the settled polyethylene slurry fromthe one or more settling legs out of the loop reactor; and flashing offthe diluent and unreacted monomers; wherein the polymerization catalystcomprises a particulate metallocene-alumoxane catalyst immobilized on aporous silica support, wherein the alumoxane is heterogeneouslydistributed on the porous silica support.